Exercise by lifelong voluntary wheel running reduces subsarcolemmal and interfibrillar mitochondrial hydrogen peroxide production in the heart

被引:108
作者
Judge, S
Jang, YM
Smith, A
Selman, C
Phillips, T
Speakman, JR
Hagen, T
Leeuwenburgh, C
机构
[1] Univ Florida, Coll Med, Dept Aging & Geriatr Res, Gen & Biomarkers Core Inst Aging,Biochem Aging La, Gainesville, FL 32608 USA
[2] Oregon State Univ, Linus Pauling Inst, Corvallis, OR 97331 USA
[3] Oregon State Univ, Dept Biochem & Biophys, Corvallis, OR 97331 USA
[4] UCL, London Ctr Res Ageing, Dept Med, Ctr Diabet & Endocrinol, London, England
[5] Univ Aberdeen, Sch Biol Sci, Ctr Energy Regulat & Obes, Aberdeen AB9 1FX, Scotland
[6] Rowett Res Inst, Div Energy Balance & Obes, Aberdeen, Scotland
关键词
aging; superoxide anion; longevity; postmitotic; calorie restriction;
D O I
10.1152/ajpregu.00396.2005
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Evidence suggests that mitochondrial dysfunction and oxidant production, in association with an accumulation of oxidative damage, contribute to the aging process. Regular physical activity can delay the onset of morbidity, increase mean lifespan, and reduce the risk of developing several pathological states. No studies have examined age- related changes in oxidant production and oxidative stress in both subsarcolemmal (SSM) and interfibrillar ( FM) mitochondria in combination with lifelong exercise. Therefore, we investigated whether long- term voluntary wheel running in Fischer 344 rats altered hydrogen peroxide (H2O2) production, antioxidant defenses, and oxidative damage in cardiac SSM and IFM. At 10 - 11 wk of age, rats were randomly assigned to one of two groups: sedentary and 8% food restriction (sedentary; n = 20) or wheel running and 8% food restriction (runners; n = 20); rats were killed at 24 mo of age. After the age of 6 mo, running activity was maintained at an average of 1,145 +/- 248 m/ day. Daily energy expenditure determined by doubly labeled water technique showed that runners expended on average similar to 70% more energy per day than the sedentary rats. Long-term voluntary wheel running significantly reduced H2O2 production from both SSM (- 10.0%) and IFM (- 9.6%) and increased daily energy expenditure (kJ/day) significantly in runners compared with sedentary controls. Additionally, MnSOD activity was significantly lowered in SSM and IFM from wheel runners, which may reflect a reduction in mitochondrial superoxide production. Activities of the other major antioxidant enzymes (glutathione peroxidase and catalase) and glutathione levels were not altered by wheel running. Despite the reduction in mitochondrial oxidant production, no significant differences in oxidative stress levels (4-hydroxy-2-nonenal- modified proteins, protein carbonyls, and malondialdehyde) were detected between the two groups. The health benefits of chronic exercise may be, at least partially, due to a reduction in mitochondrial oxidant production; however, we could not detect a significant reduction in several selected parameters of oxidative stress.
引用
收藏
页码:R1564 / R1572
页数:9
相关论文
共 64 条
[1]  
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]   Physical exercise and antioxidant defenses in the heart [J].
Atalay, M ;
Sen, CK .
HEART IN STRESS, 1999, 874 :169-177
[3]   Oxidative damage to mitochondrial DNA is inversely related to maximum life span in the heart and brain of mammals [J].
Barja, G ;
Herrero, A .
FASEB JOURNAL, 2000, 14 (02) :312-318
[4]   Endogenous oxidative stress: relationship to aging, longevity and caloric restriction [J].
Barja, G .
AGEING RESEARCH REVIEWS, 2002, 1 (03) :397-411
[5]   The quantitative measurement of H2O2 generation in isolated mitochondria [J].
Barja, G .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 2002, 34 (03) :227-233
[6]   The free radical theory of aging matures [J].
Beckman, KB ;
Ames, BN .
PHYSIOLOGICAL REVIEWS, 1998, 78 (02) :547-581
[7]   Differential responses to endurance training in subsarcolemmal and intermyofibrillar mitochondria [J].
Bizeau, ME ;
Willis, WT ;
Hazel, JR .
JOURNAL OF APPLIED PHYSIOLOGY, 1998, 85 (04) :1279-1284
[8]   Modulation of Lon protease activity and aconitase turnover during aging and oxidative stress [J].
Bota, DA ;
Van Remmen, H ;
Davies, KJA .
FEBS LETTERS, 2002, 532 (1-2) :103-106
[9]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[10]   Lifelong voluntary exercise in the mouse prevents age-related alterations in gene expression in the heart [J].
Bronikowski, AM ;
Carter, PA ;
Morgan, TJ ;
Garland, T ;
Ung, N ;
Pugh, TD ;
Weindruch, R ;
Prolla, TA .
PHYSIOLOGICAL GENOMICS, 2003, 12 (02) :129-138